Clip-N-Go Hand Sanitizers

Manufacturer
Taste Beauty LLC
Effective date
2020-09-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:13:25

Label at a glance#

ProductClip-N-Go Hand Sanitizers
Active ingredientALCOHOL
Label structure14 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Flammable.

Keep away from fire and flames.

Do Not Use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • On open skin wounds

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes, ears and mouth.
  • In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Irritation or rash occurs.

These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

OTHER SAFETY INFORMATION

  • Store between 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C(104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Denatonium Benzoate, Fragrance, PEG-40 Hydrogenated Castor Oil, Sodium Hydroxide, Water

Questions? Call:

OTC - QUESTIONS SECTION

  • 1(888)759-7870

Principal Display Panel – Fresh Scented 30 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLIP-N-GO
HAND
SANITIZER

FRESH SCENTED

1 FL OZ/30mL

Principal Display Panel – Fresh Scented 30 mL Bottle Label
Principal Display Panel – Fresh Scented 30 mL Bottle Label

Principal Display Panel – Fresh Scented 30 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLIP-N-GO
HAND
SANITIZER

FRESH SCENTED

1 FL OZ/30mL

Principal Display Panel – Fresh Scented 30 mL Bottle Label
Principal Display Panel – Fresh Scented 30 mL Bottle Label

Principal Display Panel – Fresh Scented 30 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLIP-N-GO
HAND
SANITIZER

FRESH SCENTED

1 FL OZ/30mL

Principal Display Panel – Fresh Scented 30 mL Bottle Label
Principal Display Panel – Fresh Scented 30 mL Bottle Label

Principal Display Panel – Fresh Scented 30 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLIP-N-GO
HAND
SANITIZER

FRESH SCENTED

1 FL OZ/30mL

Principal Display Panel – Fresh Scented 30 mL Bottle Label
Principal Display Panel – Fresh Scented 30 mL Bottle Label

Principal Display Panel – Fresh Scented 30 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLIP-N-GO
HAND
SANITIZER

FRESH SCENTED

1 FL OZ/30mL

Principal Display Panel – Fresh Scented 30 mL Bottle Label
Principal Display Panel – Fresh Scented 30 mL Bottle Label

Principal Display Panel – Fresh Scented 30 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CLIP-N-GO
HAND
SANITIZER

FRESH SCENTED

1 FL OZ/30mL

Principal Display Panel – Fresh Scented 30 mL Bottle Label
Principal Display Panel – Fresh Scented 30 mL Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74825-4011-12022-02-01C16284748780-1d6a99b39-e31e-a426-e053-dadaa90af4c2Drug Facts
74825-4011-12022-01-28C16284748780-1d6a99b39-e31e-a426-e053-dadaa90af4c2Drug Facts

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74825-401174825-4011-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f5f82a89-d210-484f-a3e0-9a7a8b40314ce1cf98c7-b653-4f07-b008-64e3ba27111f2022-02-01WarningsExact identifier
spl set id: e1cf98c7-b653-4f07-b008-64e3ba27111f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.